NDC 70518-4345
Methylprednisolone Sodium Succinate 125 mg injection, powder, for solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-9754.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hikma Pharmaceuticals USA Inc. names for other drugs.
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 125 mg
- Approval
- ANDA ANDA203125
- On the market since
- May 27, 2025
- Package NDCs
70518-4345-070518-4345-1- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2026
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